Composition and method for blood sugar modulation
a technology of modulation and blood sugar, applied in the direction of biocide, plant/algae/fungi/lichens, bandages, etc., can solve the problem that adults with pre-diabetes may remain in sedentary lifestyles
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example 1
[0072]A composition was prepared as shown in Table 1.
TABLE 1DosageIngredient(per 3 softgels)Gymnema Hydroethanolic extract400mgGreen Coffee Hydroethanolic extract100mgGrape Seed Aqueous extract100 mgHibiscus Hydroethanolic extract100 mgCinnamon100mgSupercritical Cinnamon−33mgHydroethanolic Cinnamon−67mgHoly Basil75 mgSupercritical Holy Basil −15mgHydroethanolic Holy Basil−60mgRussian Tarragon AQ extract50 mgGinger20mgSupercritical Ginger−3mgHydroethanolic Ginger−17mgTurmeric20mgSupercritical Turmeric−4mgHydroethanolic Turmeric−16mgGTF Chromium120mcg
[0073]In some embodiments, the composition can further include inactive ingredients, such as, for example, olive oil. In addition, or alternatively, the composition can be divided into one or more doses, such as, for example, a tablet, a pill, a capsule, a liquid, or a powder, such as, for example, a softgel capsule.
example 2
Intestinal Glucose Absorption
[0074]This example demonstrates that the ingredients shown in Example 1 can inhibit transport of glucose across the intestinal cell membrane.
[0075]Test solutions of the composition were prepared fresh on the day of use as described. Extracted herbal components equivalent to 3 supplements were solubilized in DMSO (2.44 ml) and centrifuged at 17,000×g for 5 min. Supernatants were combined to make an herbal concentrate and an aliquot (81 μl) was diluted by approximately 250 times to a final volume of 20 ml using transport buffer (pH 7.4). Sodium content was adjusted via the transport buffer, and 1 mM glucose and D-[U-14C] glucose (0.05 μCi / ml) was added The final test concentration was considered to be physiologically relevant, based on the dissolution of a normal serving of supplement in 600 ml of digestive juices. This volume was in line with reported combined volume of gastrointestinal fluid detected in the postprandial stomach (686±93 ml) and small inte...
example 3
Alpha-Glucosidase Inhibition
[0091]This example demonstrates that the ingredients shown in Example 1 can inhibit alpha-glucosidase activity.
[0092]Test solutions of the herbal composition (BSTC) were prepared in 10% DMSO solution prepared with PBS at a concentration of 10 mg / ml. Yeast (Saccharomyces cerevisiae) alpha-glucosidase purchased from Sigma was dissolved in 10 mM sodium phosphate buffer (pH 6.3) at a concentration of 0.01 U / ul. The reaction mixture was prepared by combining 10 ul of alpha-glucosidase (0.01 u / ul) and 1-20 ug / ml of the test composition in 100 ul of 10 mM phosphate buffer (pH 6.3). The positive control for alpha-glucosidase inhibition activity assay is Acarbose (200-2000 ug). The reaction mixture was warmed for 15 min in a water bath at 37° C. followed by the addition of 100 ul of 0.2 mM p-nitrophenyl-alpha-D-glucopyranoside (PNP) and further incubation at 37° C. for 30 min.
[0093]The reaction was stopped by incubating the tubes for 10 min at 100° C. in a boiling...
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